Isolation and characterization of Babesia caballi specific DNA probe and B. caballi recombinant proteins from a genomic DNA library in Lambda Zapii /

Babesia caballi DNA from infected erythrocytes was used to

Bibliographic Details
Main Author: Sahagun Ruiz, Alfredo, 1959-
Format: Thesis Book
Language:English
Published: [Place of publication not identified] : [publisher not identified] ; 1994.
Subjects:
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Description
Summary:Babesia caballi DNA from infected erythrocytes was used to
construct a genomic library in the expression vector lambda
ZAPII. Four clones expressing the same or closely related
recombinant protein were identified. The recombinant clones
contain a B.caballi insert DNA of 1.5 kDa -1.6 k]Da as
confirmed by Southern blot hybridization with biotin
labeled,B. caballi DNA. Monospecific antibody to the
recombinant protein made by antibody selection from
hyperimmune serum reacted with B. caballi antigen in IFAT and
in Western blot. The recombinant protein of approximately 55
kDa is an antigenic homologue of the 37 kDa B. caballi
antigen. The DNA insert of one of the clones Bcl, was
further characterized to develop a B. caballi specific DNA
probe. The Bcl based DNA probe hybridized to 7 ng of B.
caballi DNA but not to 3 mg of DNA from B. ecrui, B. bovis,
B. biaemina, Ana-plasma marqinale and horse white blood
cells. The B, caballi specific DNA probe identified gl
infected blood sample with 35% Restriction blood cells. The
B, caballi specific DNA probe identified B.caballi DNA from a
12.5 gl infected blood sample with 35% Pcv and 0.31%
parasitemia. Restriction enzyme experiments and Southern
blot analysis suggested that BC1 insert at least 2 times
represented in the B.Caballi genome.
Item Description:Vita.
"Major Subject: Veterinary Microbiology".
Physical Description:xiv, 87 leaves : illustrations ; 28 cm.
Issued also on microfiche from University Microfilms Inc.
Bibliography:Includes bibliographical references.